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Ethenimose

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Identification
Molecular formula
C10H13Cl2N1O3S
CAS number
51-94-9
IUPAC name
N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide
State
State

At room temperature, ethenimose is typically a solid.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
404.80
Boiling point (Kelvin)
677.95
General information
Molecular weight
271.16g/mol
Molar mass
271.1560g/mol
Density
1.8030g/cm3
Appearence

The compound generally appears as a white crystalline solid.

Comment on solubility

Solubility of N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide

N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide is a complex compound, and its solubility can be influenced by various factors, including temperature and pH. Here are some key points to consider regarding its solubility:

  • Polarity: The presence of multiple polar functional groups, such as sulfamoyl and acetamide, suggests that the compound may have polar characteristics, enhancing its ability to interact with polar solvents like water.
  • Solvent Interaction: The solubility might be significantly affected by the solvent chosen. Polar solvents may dissolve it better compared to non-polar solvents due to strong dipole interactions.
  • Temperature Dependency: As with many compounds, increasing temperature can improve solubility, so conducting experiments at varied temperatures can provide insight into its solubility profile.
  • pH Sensitivity: The compound's solubility may also vary with pH levels, which can affect ionization states of functional groups, altering solubility.

In scientific and industrial applications, understanding the solubility of N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide is crucial for predicting its behavior in different environments. Hence, conducting detailed solubility tests under various conditions will provide essential information on its effective use.

Interesting facts

Interesting Facts about N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide

N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide, often referred to by its shortened name, is a fascinating compound that has garnered attention in the field of medicinal chemistry due to its potential applications. Here are some remarkable insights into this compound:

  • Anticancer Properties: This compound is explored as a potential chemotherapeutic agent. Its structure allows for interactions that may help in targeting cancer cells effectively.
  • Mechanism of Action: The sulfamoyl functional group is important in its mechanism of action. It may inhibit enzymes such as carbonic anhydrase and has shown to interfere with the proliferation of specific tumor types.
  • Biochemical Interactions: The presence of bis(2-chloroethyl) moiety suggests that this compound can undergo nucleophilic substitution reactions, which are typical in many anticancer agents.
  • Drug Development: As researchers explore compounds like this, they focus on improving bioavailability and reducing toxicity, leading to the development of safer and more effective drugs.
  • Structure-Activity Relationship (SAR): The design of this compound highlights the importance of its functional groups. Enhancing or modifying parts of its structure could lead to variations with improved efficacy and reduced side effects.

Overall, N-[4-[bis(2-chloroethyl)sulfamoyl]phenyl]acetamide showcases the intricate relationship between chemical structure and biological activity, which is a focal point of study in drug discovery. Keep an eye on this compound as research continues, and it may lead to breakthroughs in therapeutic interventions!

Synonyms
ACETANILIDE, 4'-(BIS(2-CHLOROETHYL)SULFAMOYL)-
17262-66-7
BRN 2704944
4'-(Bis(2-chloroethyl)sulfamoyl)acetanilide
N,N-Bis(2-chloroethyl)-4-(acetylamino)benzenesulfonamide
N(sub 4)-Acetil-sulfanilil-N(sub 1)-(di-beta-cloroetil) amide [Italian]
SCHEMBL4075322
DTXSID10169359
ZZMBNTSBFXXLIU-UHFFFAOYSA-N
N(sub 4)-Acetil-sulfanilil-N(sub 1)-(di-beta-cloroetil) amide
AKOS020917965